MAP3K13[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3293012	NM_004721.5(MAP3K13):c.13C>G (p.Gln5Glu)	MAP3K13 (Q5E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472801	NM_004721.5(MAP3K13):c.44A>G (p.His15Arg)	MAP3K13 (H15R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254598	NM_004721.5(MAP3K13):c.58G>A (p.Glu20Lys)	MAP3K13 (E20K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2654329	NM_004721.5(MAP3K13):c.130G>A (p.Glu44Lys)	MAP3K13 (E44K)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2598834	NM_004721.5(MAP3K13):c.158G>A (p.Arg53Gln)	MAP3K13 (R53Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2473588	NM_004721.5(MAP3K13):c.172G>A (p.Glu58Lys)	MAP3K13 (E58K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218238	NM_004721.5(MAP3K13):c.234C>A (p.Asp78Glu)	MAP3K13 (D78E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122868	NM_004721.5(MAP3K13):c.250G>A (p.Val84Ile)	MAP3K13 (V84I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122872	NM_004721.5(MAP3K13):c.287C>T (p.Ala96Val)	MAP3K13 (A96V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3293010	NM_004721.5(MAP3K13):c.289G>T (p.Val97Leu)	MAP3K13 (V97L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122873	NM_004721.5(MAP3K13):c.311C>T (p.Thr104Met)	MAP3K13 (T104M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122874	NM_004721.5(MAP3K13):c.358T>A (p.Phe120Ile)	MAP3K13 (F120I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3122875	NM_004721.5(MAP3K13):c.511C>A (p.Leu171Met)	MAP3K13 (L171M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546274	NM_004721.5(MAP3K13):c.589G>C (p.Val197Leu)	MAP3K13 (V197L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318520	NM_004721.5(MAP3K13):c.608C>T (p.Thr203Met)	MAP3K13 (T203M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293600	NM_004721.5(MAP3K13):c.671C>T (p.Thr224Ile)	MAP3K13 (T17I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540822	NM_004721.5(MAP3K13):c.976C>T (p.Arg326Trp)	MAP3K13 (R119W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238445	NM_004721.5(MAP3K13):c.1065T>A (p.Asp355Glu)	MAP3K13 (D355E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293014	NM_004721.5(MAP3K13):c.1202G>A (p.Arg401Gln)	MAP3K13 (R194Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389416	NM_004721.5(MAP3K13):c.1246G>A (p.Ala416Thr)	MAP3K13 (A209T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122856	NM_004721.5(MAP3K13):c.1283A>C (p.Glu428Ala)	MAP3K13 (E221A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592256	NM_004721.5(MAP3K13):c.1346G>A (p.Arg449Gln)	MAP3K13 (R242Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784471	NM_004721.5(MAP3K13):c.1395G>A (p.Ala465=)	MAP3K13	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3122857	NM_004721.5(MAP3K13):c.1411C>A (p.His471Asn)	MAP3K13 (H471N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381735	NM_004721.5(MAP3K13):c.1433G>A (p.Arg478Gln)	MAP3K13 (R478Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508471	NM_004721.5(MAP3K13):c.1507C>T (p.Arg503Cys)	MAP3K13 (R296C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122858	NM_004721.5(MAP3K13):c.1550G>A (p.Arg517Gln)	MAP3K13 (R517Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122859	NM_004721.5(MAP3K13):c.1562G>A (p.Arg521His)	MAP3K13 (R314H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570010	NM_004721.5(MAP3K13):c.1576C>T (p.Pro526Ser)	MAP3K13 (P319S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3122860	NM_004721.5(MAP3K13):c.1593A>C (p.Lys531Asn)	MAP3K13 (K531N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403419	NM_004721.5(MAP3K13):c.2822C>T (p.Ser941Leu)	MAP3K13 (S734L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122871	NM_004721.5(MAP3K13):c.2839G>C (p.Asp947His)	MAP3K13 (D740H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32